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dc.contributor.authorMiki, Hirokoen_US
dc.contributor.authorYoshida, Kyousukeen_US
dc.contributor.authorKawate, Chiekoen_US
dc.contributor.authorShimada, Rintaroen_US
dc.contributor.authorTakaya, Tomohisaen_US
dc.contributor.authorIwata, Koichien_US
dc.contributor.authorHamaguchi, Hiro-oen_US
dc.date.accessioned2014-12-08T15:21:56Z-
dc.date.available2014-12-08T15:21:56Z-
dc.date.issued2012-02-27en_US
dc.identifier.issn0009-2614en_US
dc.identifier.urihttp://dx.doi.org/10.1016/j.cplett.2011.12.073en_US
dc.identifier.urihttp://hdl.handle.net/11536/15619-
dc.description.abstractPicosecond time-resolved visible absorption and Raman spectra of trans-stilbene in acetonitrile have been measured. A new transient absorption band is observed at 440 nm, whose decay time constant coincides with that of the rise of the radical cation. In addition to the known Raman bands of the radical cation, a new Raman feature showing a fast decay is found at 1599 cm(-1). We assign the 440 nm absorption band and the 1599 cm(-1) Raman band to a precursor of the radical cation. The precursor may well be an ion pair that holds an ejected electron still around the cation. (C) 2012 Elsevier B. V. All rights reserved.en_US
dc.language.isoen_USen_US
dc.titleTwo-step photoionization of trans-stilbene in acetonitrile via an ion-pair precursor studied with picosecond time-resolved absorption and Raman spectroscopiesen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/j.cplett.2011.12.073en_US
dc.identifier.journalCHEMICAL PHYSICS LETTERSen_US
dc.citation.volume527en_US
dc.citation.issueen_US
dc.citation.spage27en_US
dc.citation.epage30en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.department應用化學系分子科學碩博班zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.contributor.departmentInstitute of Molecular scienceen_US
dc.identifier.wosnumberWOS:000300614300006-
dc.citation.woscount1-
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